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- W4256383434 abstract "The odontoglossum ringspot Tobamovims (ORSV) movement and coat proteins genes were selected for the design of oligonucleotide primers for amplification of a 1,085 bp fragment. A combined assay of reverse transcription and the polymerase chain reaction (RT-PCR) was performed with 20-mer ORSV-specific primers and crude nucleic acid extracts from virus-infected orchids for rapid detection of the virus. The lowest concentration of template viral RNA required for detection was 10 fg. The RT-PCR is a 103 times more sensitive, reproducible and time-saving method than the enzyme-linked immunosorbent assay. No PCR product was observed when cymbidium mosaic potexvirus or a crude extract of healthy Cymbidium sp. were used as a template in RT-PCR with the same primers. The specificity of the primers was verified using other tobamoviruses RNAs." @default.
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- W4256383434 date "1995-11-15" @default.
- W4256383434 modified "2023-10-18" @default.
- W4256383434 title "Rapid detection and identification of odontoglossum ringspot virus by polymerase chain reaction amplification" @default.
- W4256383434 doi "https://doi.org/10.1016/0378-1097(95)00365-c" @default.
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